Mechanisms of steroid-triggered cell death in Drosophila
Mechanisms of steroid-triggered cell death in Drosophila
批准号:
6526260
负责人:
ARASH R BASHIRULLAH
金额:
$4.62万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
未结题
起止时间:
2001-09-01 至
关键词:
Drosophilidae biomarker cell death developmental genetics ecdysone fluorescence microscopy gene targeting genetic regulation genetic transcription genetically modified animals histogenesis hormone regulation /control mechanism invertebrate embryology invertebrate endocrinology larva lethal genes metamorphosis morphology morphometry mutant northern blottings organ culture reporter genes salivary glands
中文摘要
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英文摘要
DESCRIPTION (provided by applicant)
Steroid hormones are critical regulators of programmed cell death in all higher
organisms. In spite of their central role in this process, however, the
mechanisms by which steroid hormones regulate cell death remain unclear. Here,
a forward genetic strategy is proposed to study a dramatic example of
steroid-triggered cell death: the massive and rapid destruction of larval
tissues during Drosophila metamorphosis in response to the steroid hormone
ecdysone. To this end, a simple assay has been developed to monitor larval
salivary glands in living animals. Mutations that disrupt larval salivary gland
cell death will be selected and only those mutations that result in a block of
the death response, rather than those that disrupt the ecdysone signal, will be
further characterized. A genetic strategy has never been used to study
hormone-triggered cell death in any organism. These studies will provide not
only a better understanding of the hormonal regulation of programmed cell
death, but will also serve as a model system for understanding how systemic
hormonal signals are refined into stage- and tissue-specific biological
responses during development. In addition, further characterization of
apoptotic signaling pathways will allow a better understanding of autoimmune
diseases, neurodegenerative disorders, and other diseases that result from
misregulation of programmed cell death.
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